A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity.
Clicks: 454
ID: 52681
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Emerging Content
82.6
/100
454 views
301 readers
Trending
AI Quality Assessment
Not analyzed
Readership in this journal
EmergingRanked #2 of 79 articles by views in Human molecular genetics
Most read
Least read
Bar heights use a square-root scale.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Although hundreds of GWAS-implicated loci have been reported for adult obesity-related traits, less is known about the genetics specific for early-onset obesity, and with only a few studies conducted in non-European populations to date. Searching for additional genetic variants associated with childhood obesity, we performed a trans-ancestral meta-analysis of thirty studies consisting of up to 13,005 cases (≥95th percentile of BMI achieved 2-18 years old) and 15,599 controls (consistently <50th percentile of BMI) of European, African, North/South American and East Asian ancestry. Suggestive loci were taken forward for replication in a sample of 1,888 cases and 4,689 controls from seven cohorts of European and North/South American ancestry. In addition to observing eighteen previously implicated BMI or obesity loci, for both early and late onset, we uncovered one completely novel locus in this trans-ancestral analysis (nearest gene: METTL15). The variant was nominally associated in only the European subgroup analysis but had a consistent direction of effect in other ethnicities. We then utilized trans-ancestral Bayesian analysis to narrow down the location of the probable causal variant at each genome-wide significant signal. Of all the fine-mapped loci, we were able to narrow down the causative variant at four known loci to fewer than ten SNPs (FAIM2, GNPDA2, MC4R and SEC16B loci). In conclusion, an ethnically diverse setting has enabled us to both identify an additional pediatric obesity locus and further fine-map existing loci.
Abstract Quality Issue:
This abstract appears to be incomplete or contains metadata (67 words).
Try re-searching for a better abstract.
| Reference Key |
bradfield2019ahuman
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Bradfield, Jonathan P;Vogelezang, Suzanne;Felix, Janine F;Chesi, Alessandra;Helgeland, Øyvind;Horikoshi, Momoko;Karhunen, Ville;Lowry, Estelle;Cousminer, Diana L;Ahluwalia, Tarunveer S;Thiering, Elisabeth;Boh, Eileen Tai-Hui;Zafarmand, Mohammad H;Vilor-Tejedor, Natalia;Wang, Carol A;Joro, Raimo;Chen, Zhanghua;Gauderman, William J;Pitkänen, Niina;Parra, Esteban J;Fernandez-Rhodes, Lindsay;Alyass, Akram;Monnereau, Claire;Curtin, John A;Have, Christian T;McCormack, Shana E;Hollensted, Mette;Frithioff-Bøjsøe, Christine;Valladares-Salgado, Adan;Peralta-Romero, Jesus;Teo, Yik-Ying;Standl, Marie;Leinonen, Jaakko T;Holm, Jens-Christian;Peters, Triinu;Vioque, Jesus;Vrijheid, Martine;Simpson, Angela;Custovic, Adnan;Vaudel, Marc;Canouil, Mickaël;Lindi, Virpi;Atalay, Mustafa;Kähönen, Mika;Raitakari, Olli T;van Schaik, Barbera D C;Berkowitz, Robert I;Cole, Shelley A;Voruganti, V Saroja;Wang, Yujie;Highland, Heather M;Comuzzie, Anthony G;Butte, Nancy F;Justice, Anne E;Gahagan, Sheila;Blanco, Estela;Lehtimäki, Terho;Lakka, Timo A;Hebebrand, Johannes;Bonnefond, Amélie;Grarup, Niels;Froguel, Philippe;Lyytikäinen, Leo-Pekka;Cruz, Miguel;Kobes, Sayuko;Hanson, Robert L;Zemel, Babette S;Hinney, Anke;Teo, Koon K;Meyre, David;North, Kari E;Gilliland, Frank D;Bisgaard, Hans;Bustamante, Mariona;Bonnelykke, Klaus;Pennell, Craig E;Rivadeneira, Fernando;Uitterlinden, André G;Baier, Leslie J;Vrijkotte, Tanja G M;Heinrich, Joachim;Sørensen, Thorkild I A;Saw, Seang-Mei;Pedersen, Oluf;Hansen, Torben;Eriksson, Johan;Widén, Elisabeth;McCarthy, Mark I;Njølstad, Pål R;Power, Christine;Hyppönen, Elina;Sebert, Sylvain;Brown, Christopher D;Järvelin, Marjo-Riitta;Timpson, Nicholas J;Johansson, Stefan;Hakonarson, Hakon;Jaddoe, Vincent W V;Grant, Struan F A;, ; |
| Journal | Human molecular genetics |
| Year | 2019 |
| DOI |
ddz161
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.